安非他酮
抗抑郁药
文拉法辛
再摄取抑制剂
米氮平
奈法唑酮
药理学
三环
5-羟色胺能
血清素
再摄取
去甲肾上腺素
西酞普兰
5-羟色胺摄取抑制剂
雷波西汀
精神药理学
心理学
医学
氟西汀
多巴胺
神经科学
内科学
受体
戒烟
病理
海马体
出处
期刊:PubMed
日期:1998-01-01
卷期号:59 Suppl 4: 5-14
被引量:153
摘要
Distinct pharmacologic mechanisms allow the antidepressants to be separated into seven different classes. These basic pharmacologic concepts can explain not only the therapeutic actions, but also the side effects of the wide range of antidepressants currently available. The two classical mechanisms are those of tricyclic antidepressants (TCAs) and monoamine oxidase inhibitors (MAOIs). The most widely prescribed agents are the serotonin selective reuptake inhibitors (SSRIs). Three other classes of antidepressants, like the SSRIs, increase serotonergic neurotransmission, but they also have additional actions, namely dual serotonin and norepinephrine reuptake inhibition (venlafaxine); serotonin-2 antagonism/reuptake inhibition (nefazodone); and alpha2 antagonism plus serotonin-2 and -3 antagonism (mirtazapine). The selective norepinephrine and dopamine reuptake inhibitor bupropion defines a novel class of antidepressant that has no direct actions on the serotonin system.
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